Canonical Allele Identifier: CA696955790

Gene: RPL21

Linked Data

• dbSNP Id: rs1422803018
• MyVariant Identifiers: chr13:g.27828063_27828064del (hg19) ; chr13:g.27253926_27253927del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27253929_27253930del , CM000675.2:g.27253929_27253930del	GRCh38
NC_000013.10:g.27828066_27828067del , CM000675.1:g.27828066_27828067del	GRCh37
NC_000013.9:g.26726066_26726067del	NCBI36
NG_046927.1:g.7375_7376del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.67+86_67+87del MANE Select	ENSP00000346027.4:n.67+86_67+87del
ENST00000272274.8:c.67+86_67+87del	ENSP00000351021.2:n.67+86_67+87del
ENST00000311549.10:c.67+86_67+87del	ENSP00000346027.4:n.67+86_67+87del
ENST00000319826.8:c.67+86_67+87del	ENSP00000370574.1:n.67+86_67+87del
ENST00000326092.8:c.67+86_67+87del	ENSP00000370569.1:n.67+86_67+87del
ENST00000461690.5:c.67+86_67+87del	ENSP00000434298.1:n.67+86_67+87del
ENST00000466550.1:n.79+86_79+87del
ENST00000473558.5:n.303+86_303+87del
ENST00000483765.5:c.67+86_67+87del	ENSP00000473246.1:n.67+86_67+87del
ENST00000493317.1:c.67+86_67+87del	ENSP00000471695.1:n.67+86_67+87del
NM_000982.3:c.67+86_67+87del	NP_000973.2:n.67+86_67+87del
NM_000982.4:c.67+86_67+87del MANE Select	NP_000973.2:n.67+86_67+87del